This report is to describe a case of a rare autosomal dominant genodermatosis known as Huriez syndrome in a 41 year-old female patient presenting with recurrent skin lesions. Following investigations, the patient was diagnosed to have Huriez syndrome. She was planned for excision and follow up in the plastic surgery, dermatology and oncology departments.
Huriez syndrome, also known as ‘sclerotylosis’ a rare autosomal dominant genodermatosis which has been first reported in France by Huriez et al. later it has been reported in India, Japan, Tunisia Germany, ðtaly and Turkey.
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